CAS 1138-80-3
:N-Carbobenzyloxyglycine
Description:
N-Carbobenzyloxyglycine, also known as Cbz-Gly, is an amino acid derivative characterized by the presence of a carbobenzyloxy (Cbz) protecting group attached to the amino group of glycine. This compound typically appears as a white to off-white crystalline solid and is soluble in organic solvents such as methanol and dichloromethane, but less soluble in water. The Cbz group serves as a protective moiety, making N-Carbobenzyloxyglycine useful in peptide synthesis, as it can be selectively removed under specific conditions to yield the free amino acid. The compound is often utilized in organic synthesis and medicinal chemistry, particularly in the development of peptide-based drugs. Its molecular structure includes a glycine backbone, which contributes to its role in biological systems, and the Cbz group enhances its stability and reactivity in various chemical reactions. As with many chemical substances, proper handling and safety precautions are essential due to potential hazards associated with its use.
Formula:C10H11NO4
InChI:InChI=1/C10H11NO4/c12-9(13)6-11-10(14)15-7-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,11,14)(H,12,13)/p-1
InChI key:InChIKey=CJUMAFVKTCBCJK-UHFFFAOYSA-N
SMILES:C(OC(NCC(O)=O)=O)C1=CC=CC=C1
Synonyms:- (Carbobenzoxy)glycine
- (Carbobenzyloxy)glycine
- 2-(Benzyloxycarbonylamino)acetic acid
- 2-(Phenylmethoxycarbonylamino)acetic acid
- Benzyloxycarbonylglycine
- Cbz-Gly-OH
- Cbz-glycine
- Glycine, N-[(phenylmethoxy)carbonyl]-
- Glycine, N-carboxy-, N-benzyl ester
- N-(Benzyloxycarbonyl)glycine
- N-(Carbobenzoxy)glycine
- N-(Carbobenzyloxy)glycine
- N-(α-Carbobenzoxy)glycine
- N-Benzyloxycarbonylglycin
- N-Benzyloxycarbonylglycine
- N-CBZ-Glycine N-Carbobenzyloxy-glycine
- N-Carboxyglycine N-benzyl ester
- N-Cbz-Gly-OH
- N-Cbz-glycine
- N-[(Phenylmethoxy)carbonyl]glycine
- N-[(benzyloxy)carbonyl]glycine{[(benzyloxy)carbonyl]amino}acetate
- N-benciloxicarbonilglicina
- N-cbz-glycine crystalline
- N<sup>α</sup>-(Benzyloxycarbonyl)glycine
- Nsc 2526
- Nα-(Benzyloxycarbonyl)glycine
- Z-Gly-OH
- Z-glycine
- [[(Benzyloxy)carbonyl]amino]acetic acid
- z-Gly
- RARECHEM AL BO 0395
- N-CARBOBENZOXYGLYCINE
- Z-L-GLYCINE
- CBZ-GLY
- CARBOBENZYLOXYGLYCINE
- N-ALPHA-BENZYLOXYCARBONYL-GLYCINE
- N-CBZ-GLYCINE-OH
- N-ALPHA-CBZ-GLYCINE
- N-ALPHA-CARBOBENZOXY-GLYCINE
- 2-([(BENZYLOXY)CARBONYL]AMINO)ACETIC ACID
- LABOTEST-BB LT00005891
- BENZYLOXYCARBONYL-GLYCINE
- TIMTEC-BB SBB003458
- See more synonyms
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Found 13 products.
N-Carbobenzoxyglycine
CAS:Formula:C10H11NO4Purity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:209.20N-Benzyloxycarbonylglycine, 98+%
CAS:<p>N-Carbobenzoxyglycine is used in the dipeptide synthesis. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has n</p>Formula:C10H11NO4Purity:98+%Color and Shape:Crystals or powder or crystalline powder, WhiteMolecular weight:209.20Z-Gly-OH
CAS:<p>Bachem ID: 4000228.</p>Formula:C10H11NO4Purity:98.8%Color and Shape:WhiteMolecular weight:209.2Glycine, N-[(phenylmethoxy)carbonyl]-
CAS:Formula:C10H11NO4Purity:95%Color and Shape:SolidMolecular weight:209.1986Z-Glycine
CAS:<p>N-Benzyloxycarbonylglycine is a lipid-like drug designed for enhanced brain penetration.</p>Formula:C10H11NO4Purity:99.88%Color and Shape:Slightly Beige PowderMolecular weight:209.2N-Carbobenzoxyglycine
CAS:<p>Applications N-Carbobenzoxyglycine is used in the dipeptide synthesis.<br>References Hans, D., et al.: Med. Chem., 2, 627 (2006), Guzman, F., et al.: J. Biotechnol., 10, 279 (2007), Vlieghe, P., et al.: Drug Discov. Today, 15, 40 (2010),<br></p>Formula:C10H11NO4Color and Shape:NeatMolecular weight:209.2Cbz-glycine
CAS:<p>Cbz-glycine is a hydrogen bond donor that can react with trifluoroacetic acid in a one-step reaction to form an ester hydrochloride. It is used in the synthesis of monoclonal antibodies and has been shown to inhibit the growth of receptor cells. Cbz-glycine reacts with protocatechuic acid, pyrazinoic acid, and ester hydrochloride to form pharmacokinetic properties. It has been shown to have pharmacokinetic properties by inhibiting prostaglandin synthesis.</p>Formula:C10H11NO4Purity:Min. 95%Molecular weight:209.2 g/molZ-Gly-OH
CAS:<p>M03051 - Z-Gly-OH</p>Formula:C10H11NO4Purity:95%Color and Shape:Solid, White to off-white crystalline powderMolecular weight:209.201Z-Glycine extrapure, 99%
CAS:Formula:C10H11NO4Purity:min. 99 %Color and Shape:White, Crystalline powderMolecular weight:209.2











